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Effect of the Expression of the Human pub Gene on the Proliferation and Differentiation of Rat Pheochromocytoma PC-12 Cells

机译:人pub基因表达对大鼠嗜铬细胞瘤PC-12细胞增殖和分化的影响

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摘要

We studied the effect of overexpression of the human pub gene on the proliferation and neuronal differentiation of PC-12 cells treated with nerve growth factor. We obtained a stable cell line overexpressing the human pub gene (the PC12-hpub line) and PC12-DNA3 control cell line. Using reverse transcription PCR, we showed transgene expression in cells of the PC12-hpub line. We found that under standard culturing conditions and under conditions of deprivation of trophic factors (1% embryonic calf serum), the growth rate of PC12-hpub cells did not differ from the rate of control PC12-DNA3 cells. After the induction of differentiation in these cells lines using nerve growth factor in the absence of serum, we found that, in 5 days, the number of differentiated cells with the neuronal phenotype in the PC12-hpub cells was smaller by a factor of 5 as compared to the control PC12-DNA3 cells. Thus, overexpression of the human pub gene in rat pheochromocytoma PC12 cells led to the suppression of their nerve-growth-factor-induced differentiation.
机译:我们研究了人类pub基因的过表达对神经生长因子治疗的PC-12细胞增殖和神经元分化的影响。我们获得了稳定表达人pub基因的稳定细胞系(PC12-hpub系)和PC12-DNA3对照细胞系。使用逆转录PCR,我们显示了PC12-hpub系细胞中的转基因表达。我们发现,在标准培养条件下和在缺乏营养因子(1%胚胎小牛血清)的条件下,PC12-hpub细胞的生长速度与对照PC12-DNA3细胞的生长速度没有差异。在不存在血清的情况下使用神经生长因子诱导这些细胞系分化后,我们发现,在5天内,PC12-hpub细胞中具有神经元表型的分化细胞数量减少了5倍。与对照PC12-DNA3细胞相比。因此,人pub基因在大鼠嗜铬细胞瘤PC12细胞中的过表达导致其神经生长因子诱导的分化受到抑制。

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